Functional Insights in PLS3-Mediated Osteogenic Regulation.
actin-bundling protein
osteogenic differentiation
osteoporosis
plastin-3
transcriptome
Journal
Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052
Informations de publication
Date de publication:
09 Sep 2024
09 Sep 2024
Historique:
received:
15
07
2024
revised:
26
07
2024
accepted:
29
07
2024
medline:
14
9
2024
pubmed:
14
9
2024
entrez:
14
9
2024
Statut:
epublish
Résumé
Plastin-3 (PLS3) encodes T-plastin, an actin-bundling protein mediating the formation of actin filaments by which numerous cellular processes are regulated. Loss-of-function genetic defects in PLS3 are reported to cause X-linked osteoporosis and childhood-onset fractures. However, the molecular etiology of PLS3 remains elusive. Functional compensation by actin-bundling proteins ACTN1, ACTN4, and FSCN1 was investigated in zebrafish following morpholino-mediated
Identifiants
pubmed: 39273077
pii: cells13171507
doi: 10.3390/cells13171507
pii:
doi:
Substances chimiques
plastin
0
Microfilament Proteins
0
Membrane Glycoproteins
0
Zebrafish Proteins
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Deutsche Forschungsgemeinschaft
ID : FOR2722
Organisme : Guangdong Province Basic and Applied Basic Research Fund Project
ID : 2022A1515011121
Organisme : Guangzhou Elite Project
ID : JY202028